Kumano Gaku, Ezal Carin, Smith William C
Department of Molecular, Cellular and Developmental Biology, University of California, Santa Barbara, CA 93106, USA.
Dev Biol. 2006 Nov 15;299(2):411-23. doi: 10.1016/j.ydbio.2006.08.010. Epub 2006 Aug 10.
We describe here the cloning of a new member of the TGF-beta family with similarity to the anti-dorsalizing morphogenetic proteins (ADMPs). This new gene, ADMP2, is expressed in a broad band of mesendoderm cells that appear to include the progenitors of the endoderm and the ventral mesoderm. Antisense morpholino oligonucleotide knockdown of ADMP2 results in near-complete disruption of primitive blood and heart development, while the development of other mesoderm derivatives, including pronephros, muscle and lateral plate is not disrupted. Moreover, the development of the primitive blood in ADMP2 knockdown embryos cannot be rescued by BMP. These results suggests that ADMP2 plays an early role in specifying presumptive ventral mesoderm in the leading edge mesoderm, and that ADMP2 activity may be necessary to respond to BMP signaling in the context of ventral mesoderm induction.
我们在此描述了一种与抗背化形态发生蛋白(ADMPs)相似的TGF-β家族新成员的克隆。这个新基因ADMP2在中内胚层细胞的一条宽带中表达,这些细胞似乎包括内胚层和腹侧中胚层的祖细胞。ADMP2的反义吗啉代寡核苷酸敲低导致原始血液和心脏发育几乎完全中断,而其他中胚层衍生物(包括前肾、肌肉和侧板)的发育未受干扰。此外,BMP不能挽救ADMP2敲低胚胎中原始血液的发育。这些结果表明,ADMP2在确定前缘中胚层中假定的腹侧中胚层方面起早期作用,并且在腹侧中胚层诱导的背景下,ADMP2活性可能是响应BMP信号所必需的。